目的：探讨葡萄胎染色体分析的临床意义。
Objective: To explore the clinical significance of chromosomal analysis of hydatidiform mole.
方法绒毛细胞培养法及G显带制作染色体分析。
Methods Use villus cell culture and the chromosome with G-bands by trypsin using Giemsa.
血象检查采用常规法，染色体分析采用微量全血培养法。
Hemograms were analyzed by routine method, chromosome were examined using the whole blood of tiny culture method.
染色体分析以超二倍体为主，核型显示为人类染色体核型。
Chromosomal analysis of the tumor cells exhibited human origin with a hyperdiploid model.
方法：对756例遗传咨询者进行外周血淋巴细胞染色体分析。
Methods: The chromosomes were obtained by culturing peripheral blood lymph cells collected from 756 cases for genetic counseling.
目的通过对患者外周血染色体分析，探讨染色体异常与疾病的关系。
Objective: To study the relationship between the abnormal karyotype and the disease with karyotype analysis.
对所得阳性杂交瘤细胞作染色体分析并对单克隆抗体进行特性分析。
The chromosome of the positive hybridoma and the character of the mAb were analysed.
在细胞遗传学的临床与科学研究中，染色体分析是一项很重要的任务。
During the clinical and scientific research of cell genetics, the analysis of chromosome is an important task.
结论对于不明原因的自然流产夫妇，染色体分析应作为常规的检测方法。
Conclusion: Chromosomal analysis should be carried out routinely in couples with unexplained failure of reproduction.
引言染色体分析是临床诊断、诱变因素剂量学和生物学研究的一个重要而困难的任务。
Chromosome analysis is an important and difficult task in clinical diagnosis, mutagen dosimetry and biological research.
结论儿童aml进行染色体分析及融合基因的检测，有助于AML诊断及亚型之间的鉴别诊断。
Conclusion Chromosome analysis and detection of fusion genes are helpful in the diagnosis of AML and the differentiation diagnosis of AML subtype.
应用氯化镉致人胚肺成纤维细胞恶性转化实验、染色体分析、流式细胞术对氯化镉的致癌机理进行研究。
The mechanism of carcinogenesis induced by CdCl 2 was studied through experiments of the malignant transformation of human embryo lung fibroblast in vitro, chromosome analysis and flow cytometry.
DNA分析也显示仅仅一个染色体的一小部分被转移。
The DNA analyses also show that only a small part of a chromosome was transferred.
自动化dna分析在诸如染色体作图，基因组测序以及DNA、RNA与蛋白质互作这类领域的应用潜力巨大。
Automated DNA synthesis has been essential in such fields as chromosome mapping, genomic sequencing and the study of interactions between DNA, RNA and proteins.
目前，研究人员正在分析这种疾病的染色体结构，并已识别出它的染色体组型。
The team is working on the disease's chromosome structure and has just identified the karyotype. (Karyotypes are pictures of cellular chromosomes that are used to check for abnormalities.)
随后的染色体组分析显示，被改造细菌的DNA中存在大量的变异。
Subsequent genome analysis revealed numerous mutations in the DNA of the adapted bacteria.
一种叫微阵列(microarray)的新仪器，即一块覆盖着DNA序列的小芯片，可以同时分析染色体上的很多点。
A new device called the microarray, a small chip coated with DNA sequences, can simultaneously analyze many more spots on the chromosomes.
目前染色体畸变分析方法主要包括常规染色法、G显带法和FISH技术等。
The methods of analysis of the chromosome aberrations mainly include routine staining method, G-banding method and FISH technique.
结论FISH是一种在分析CLL染色体数目和结构异常方面较为快速、准确和敏感的方法，可为CLL的研究提供较为准确的分子遗传学信息。
Conclusion FISH is a more rapid, accurate and sensitive technique in analysis of chromosome aberrations in CLL. FISH may provide accurate information of molecular cytogenetics for CLL.
另外的一些人希望更多了解自己：一个团体叫DIYgenomics团结一致了分析他们的染色体组，甚至进行和参与小临床试验。
Others hope to learn more about themselves: a group called DIYgenomics has banded together to analyse their genomes, and even conduct and participate in small clinical trials.
由于拥有先进的基因序列分析技术和获得冰岛人基因资料的特权。DeCodeGenetics公司在个人染色体领域处于领先地位。
By combining advanced gene-sequencing technologies with privileged access to the genetic data of Icelanders, DeCode Genetics pioneered the field of personal genomics.
这些都是染色体组型分析方法的改进。
通过对血液样本的分析，Samani教授和Spector教授发现，有些人具有与其年龄不相称的过短染色体端粒，而一种特定的基因序列在这些人中更常见。
From blood samples, Samani and Spector found a particular gene sequence was more common in people who had unusually short telomeres for their age.
这是用来分析染色体组成的女性。
This is used to analyse the chromosomal composition of the female.
结合这两个种的染色体倍性鉴定、序列分析和栽培观察实验，初步确定划分为两个种。
Acoording the ploidy analysis of chromosome, sequences and the survey of cultivation in field, Opisthopappus is primarily divided into two species.
全部染色体进行测量分析，计算相对长度和双臂染色体着丝粒指数。
The chromosomes were measured and analysed on the basis of their relative length and centromere index.
结论染色体畸变分析是非常可靠的生物剂量估算方法。
Conclusion The analysis of chromosomal aberrations is an extremely reliable method in biological dosimetry.
本文以小鼠精原细胞染色体畸变分析方法研究其对雄性生殖细胞的诱变性。
The mutagenicity of avermectin on male germ cells was studied by the method of analysis of chromosomal aberrations in mouse spermatogonia.
本文以小鼠精原细胞染色体畸变分析方法研究其对雄性生殖细胞的诱变性。
The mutagenicity of avermectin on male germ cells was studied by the method of analysis of chromosomal aberrations in mouse spermatogonia.
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